• accession：NM_001077620
• 基因别名：PRCD
• 基因描述：Homo sapiens progressive rod-cone degeneration (PRCD), transcript variant 1, mRNA.
• 载体：现货载体
• CDS区长度：165
• 翻译后氨基酸长度：54
• TranscriptVariant：This variant (1) represents the protein coding transcript.
• 基因简介：This gene is predominantly expressed in the retina, and mutations in this gene are the cause of autosomal recessive retinal degeneration in both humans and dogs. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2010]
• 载体信息：自有图片地址
• 规格：10ul 质粒

CDS区参考序列： 点击查看序列

ATGTGCACCACCCTTTTCCTGCTCAGCACCCTGGCCATGCTCTGGCGCCGCCGATTTGCCAACCGAGTCCAACCAGAGCCCAGCGACGTGGATGGGGCAGCTAGGGGCAGCAGCTTGGATGCGGACCCTCAGTCCTCAGGCAGGGAGAAAGAACCTCTGAAGTAA

翻译后氨基酸参数序列： 点击查看序列

ATGTGCACCACCCTTTTCCTGCTCAGCACCCTGGCCATGCTCTGGCGCCGCCGATTTGCCAACCGAGTCCAACCAGAGCCCAGCGACGTGGATGGGGCAGCTAGGGGCAGCAGCTTGGATGCGGACCCTCAGTCCTCAGGCAGGGAGAAAGAACCTCTGAAGTAA